US1528255A - Hydrolysis of sulphuryl chloride - Google Patents
Hydrolysis of sulphuryl chloride Download PDFInfo
- Publication number
- US1528255A US1528255A US710157A US71015724A US1528255A US 1528255 A US1528255 A US 1528255A US 710157 A US710157 A US 710157A US 71015724 A US71015724 A US 71015724A US 1528255 A US1528255 A US 1528255A
- Authority
- US
- United States
- Prior art keywords
- sulphuryl chloride
- tower
- acid
- steam
- hydrolysis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/69—Sulfur trioxide; Sulfuric acid
- C01B17/74—Preparation
Definitions
- This invention relates to sulphuryl chloride to produce sulfuric acid and hydrochloricacid.
- Any acid-proof tower of the general type of that used for the Glover tower of .ajsulfuric acid plant may be employed and it .is filled-with the usual, tower filling.
- the sulphuryl chloride and steam are introduced in the bottom of the tower in the proportions wished, e.' g., one volume oflsulphuryl chloride vapor to four volumes of steamL
- the steam may be slightly superheated to a temperature between 250 'and 300 F.
- a tower of-the usual acid proof construction and of any desiped height, for instance, 25 feet, may be. employed.
- This tower is filled with any of theusual tower filling and sulphuryl chloride and steam, which may be superheated, is introduced into the bottom of thetower. .
- steam which may be superheated, is introduced into the bottom of thetower.
- Some of the steam first introduced will condense in the tower, giving the desired water to form a catalyst in the hydrolysis of the sulphuryl chloride.
- the sulfuric acid will be formed throughout the tower and will be dilute, dueto the presence of an excess quantity of water. This acid will flow downwardly through the upwardly passing vapors and the sulphuryl chloride will react on the water contained in the dilute acid formin additional sulfuric acid.
- the sudfurio aci of the tower is of approximately 80 per cent strength and may be cooled and shipped in the ordinary manner.
- the vapors may be con ensed to flowing from the bottom produce muriatic acid of a purity comparing with the commercial muriatic acid on' tower, the hot burner gases thereof, a more concentrated sulfuric acid may be Obtained;
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
I Patented Mar. 3, 1925.
v To all whom it may concern:
UNITED: STATES.
miner: 11. Manna-or new YORK, n. Y.
EYDRQLYSIS or suLrHuaYr. CELORIDE.
No Drawing.
Be it' known that I, RALPH H. MCKE El, a citizen of the United States,'res1ding at New .York, in the county of New York and State of New York, have invented certain 1- new and useful Improvements in Hydrolysis of sulphuryl Chloride, of which the following-is a speci cation.
This invention relates to sulphuryl chloride to produce sulfuric acid and hydrochloricacid.
It has heretofore been proposed to produce sulfuric acid of from 65 to 80 per cent strength and gaseous hydrogen chloride by bringing together chlorine, sulfur dioxid, and steam for water or dilutehydrochloric acid -in a reaction tower. This process is open to several objections, one of which is the necessity of carefully regulating the proportions of chlorine and sulfur dioxid. The
'use of a small excess of either substance permits alarge amount of the inertmixed gas to escape from the tower and thereby causes a decided loss in yield and creates a nuisance 1n the community in which the process is being carried out.
It'is also impracticalto shipachlcirine gas and sulfurdioxid gas to a plant for tlie purpose of practicing this processfand it is, therefore, necessary to make these gases at the point where they\a e to be used.
The shipment of large amounts of hydro' chloric acid is also very expensive due to the large amount of water which has to be transported therewith and the cost of the containers in which the acid is shipped.
By combining sulfur dioxid and chlorine to produce sulphuryl chloride in the manner described and claimed in my prior application filed June 26, 1923, Serial No. M7599, and then shipping the sulphuryl chloride to the point where the sulfuric acid and the hydrochloric acid are to c be manufactured, these disadvantages may be overcome, as sulphuryl chloride may be easily shipped in tank cars or metal drums.
. The hydrolysis of sulphuryl chloride by -the use of an excess of water has been proposed, but the concentration of the sulfuric acid obtained in this manner is small and the hydrochlorid acid formed is mixed with" hydrolysis of Application filed April 30, 1924. Serial No. 719,157.
and sulphuryl chloride will not reactto form sulfuric acid and hydrogen chloride, I have found that theuse of a catalyst and particularly the use of a small amount of water causes areaction to take placerapidly. Any acid-proof tower of the general type of that used for the Glover tower of .ajsulfuric acid plant may be employed and it .is filled-with the usual, tower filling. The sulphuryl chloride and steam are introduced in the bottom of the tower in the proportions wished, e.' g., one volume oflsulphuryl chloride vapor to four volumes of steamL The steam may be slightly superheated to a temperature between 250 'and 300 F. When the steam is first introduced into a tower at ordinary temperature, some of the moisture will be condensed on the Walls of the tower or the filling and start the reaction. Dilute sulfuric acid will be formed in the upper part of the tower and flow downwardly; being concentrated by the reaction of the sulphuryl chloride on the water contained in the dilute acid. The hot sulfuric acid of about 80 per cent strength will flow from the bottom of the tower, and after cooling may be shipped in the-ordinary way.
In a typical embodiment of the invention, a tower of-the usual acid proof construction and of any desiped height, for instance, 25 feet, may be. employed. This tower is filled with any of theusual tower filling and sulphuryl chloride and steam, which may be superheated, is introduced into the bottom of thetower. .Some of the steam first introduced will condense in the tower, giving the desired water to form a catalyst in the hydrolysis of the sulphuryl chloride. The sulfuric acid will be formed throughout the tower and will be dilute, dueto the presence of an excess quantity of water. This acid will flow downwardly through the upwardly passing vapors and the sulphuryl chloride will react on the water contained in the dilute acid formin additional sulfuric acid. The sudfurio aci of the tower is of approximately 80 per cent strength and may be cooled and shipped in the ordinary manner. i The hydrogen chloride gas'passes from the top of the tower together with some The process should be so regulated that no sulphuryl chloride or only traces of sulphurylchloride Will'escape from the to of the tower. The vapors may be con ensed to flowing from the bottom produce muriatic acid of a purity comparing with the commercial muriatic acid on' tower, the hot burner gases thereof, a more concentrated sulfuric acid may be Obtained;
When the sulfuric acid is concentrated by heating in vthe tower, a product of more than 90 er cent strength is obtained.
lVhile I have described in detail the preferred practice of my process, it is to be understood that the details of procedure, and
' proportion of ingredients may be widely varied, and that knownch emlcal equivalents .joined claims.
may be employed in place of the materials mentioned, without departing fromthe splrit of the invention or'the scope of the sub- 1 claim:-
1. The process of hydrolyzing sulphuryl chloride which compr1sestreating sulphuryl chloride vapor with steam in the presence of a catalyst.
2. The process of hydrolyzing sulphuryl chloride which comprises treating sulphuryl chloridevapor with steam inthe presence of water.
3. The process of hydrolyzing sulphuryl chloride whichcomprises passing sulphuryl chloride Vapor. and steam upwardly through an acid tower. i
4. The process of hydrolyzing sulphuryl chloride which comprises contacting sulphuryl chloride vapor and steam, and;permitting some of the steam to" condense whereby the water formed will serve as a catalyst to .cause the sulphuryl chloride and steam to react with each other. e
5. The process of hydrolyzing sulphuryl chloride which comprises passing sulphuryl chloride gas and dry steam upwardly through a tower, delivering heated gases to the tower, and concentrating the sulfuric acid formed. 7
In testimony whereof, I afiix my signature in presence of two .witnesses.
, RALPH H. McKEE.
-Witnesses:
DONALDE. CABLE,
' MARGARET J. STONE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US710157A US1528255A (en) | 1924-04-30 | 1924-04-30 | Hydrolysis of sulphuryl chloride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US710157A US1528255A (en) | 1924-04-30 | 1924-04-30 | Hydrolysis of sulphuryl chloride |
Publications (1)
Publication Number | Publication Date |
---|---|
US1528255A true US1528255A (en) | 1925-03-03 |
Family
ID=24852850
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US710157A Expired - Lifetime US1528255A (en) | 1924-04-30 | 1924-04-30 | Hydrolysis of sulphuryl chloride |
Country Status (1)
Country | Link |
---|---|
US (1) | US1528255A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2871098A (en) * | 1955-07-19 | 1959-01-27 | Technical Entpr Inc | Production of hydrogen chloride and sulfuric acid |
US3492091A (en) * | 1967-08-02 | 1970-01-27 | Stauffer Chemical Co | Production of aqueous or anhydrous hydrogen chloride free of sulfur dioxide |
-
1924
- 1924-04-30 US US710157A patent/US1528255A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2871098A (en) * | 1955-07-19 | 1959-01-27 | Technical Entpr Inc | Production of hydrogen chloride and sulfuric acid |
US3492091A (en) * | 1967-08-02 | 1970-01-27 | Stauffer Chemical Co | Production of aqueous or anhydrous hydrogen chloride free of sulfur dioxide |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB367660A (en) | Process for the production of ammonium nitrate | |
US1528255A (en) | Hydrolysis of sulphuryl chloride | |
US1562914A (en) | Process for producing carbon and hydrocyanic acid | |
US1480166A (en) | Manufacture of hydrazine | |
US2014374A (en) | Ammonia recovery | |
GB799624A (en) | Slurry process for the manufacture of hydrogen fluoride | |
US1943345A (en) | Recovery of ammonia from cook liquor | |
US1901416A (en) | Production of gaseous mixtures containing sulphur dioxide | |
US1229509A (en) | Process of manufacture of hydrochloric acid. | |
US1982407A (en) | Process of producing hydrogen cyanide | |
US2139721A (en) | Concentration of nitric acid | |
US1777025A (en) | Method of manufacturing chemically-pure sulphuric acid | |
US3812242A (en) | Process for the simultaneous production of sulphur dioxide and concentrated aqueous sulphuric acid | |
US2021791A (en) | Process for producing hydrated ferric chloride | |
US2007478A (en) | Production of nitrates from metal halides | |
US2123072A (en) | Process for the treatment of gases | |
US1031864A (en) | Method of concentrating nitric acid. | |
US1185029A (en) | Process for the manufacture of sulfuric acid. | |
US2208112A (en) | Process for producing a metal nitrate and chlorine from nitric acid and a metal chloride | |
US2138016A (en) | Process for the production of a nitrate and chlorine | |
US1616703A (en) | Method for cooling and utilizing the heat content of relief gas from sulphite digesters | |
GB438541A (en) | Improvement in production of alkali and alkaline earth metal nitrates | |
US1922278A (en) | Process of concentrating nitric acid | |
US1133086A (en) | Production of ammonium sulfate. | |
US2138017A (en) | Process for the decomposition of nitrosyl chloride |